Tyco Healthcare Deutschaland GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Tyco Healthcare Deutschaland GmbH makes
Tyco Healthcare Deutschland GmbH manufactures the RESPIFLO, a respiratory therapy device designed for mechanical ventilation and oxygen therapy in clinical settings.
The RESPIFLO is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Respiflo Ref K962872
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tyco Healthcare Deutschaland GmbH have in the registry?
The registry currently lists 1 device for Tyco Healthcare Deutschaland GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tyco Healthcare Deutschaland GmbH's devices?
Among its 1 most recently registered device, Tyco Healthcare Deutschaland GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Tyco Healthcare Deutschaland GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tyco Healthcare Deutschaland GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tyco Healthcare Deutschaland GmbH in the registry?
The most recently registered devices listed for Tyco Healthcare Deutschaland GmbH include RESPIFLO.